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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246804Generated: October 31, 2026

Acetic Acid → 1-(Diphenylmethyl)-3-(methylamino)-3-azetidinecarbonitrile

https://huagongshe.com/reaction/1246804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium CyanideHCID 9032—
Reactant1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventMethanolHCID 887—
Product1-(Diphenylmethyl)-3-(methylamino)-3-azetidinecarbonitrileHCID 21905775—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-benzhydrylazetidin-3-one (2.13 g, 8.98 mmol) in methanol (17 ml) was added methylamine hydrochloride (1.21 g, 18.0 mmol) and then acetic acid (1.03 ml, 18.0 mmol) at room temperature. After stirring for 5 minutes, solid KCN (1.17 g, 18.0 mmol) was added and the mixture was heated to 60° C. for 19 hours. The reaction was cooled; the solid product was collected by vacuum filtration, rinsed with methanol, and then dried, in vacuo, to afford I-(29A-7)a as a colorless solid (2.50 g, quantitative): +ES MS (M+1) 278.3; 1H NMR (400 MHz, CD2Cl2) δ 7.43 (d, J=7.5 Hz, 4H), 7.29 (t, J=7.5 Hz, 4H), 7.23 (t, J=7.3 Hz, 2H), 4.45 (s, 1H), 3.55 (d, J=7.5 Hz, 2H), 3.15 (d, J=7.1 Hz, 2H), 2.40 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129239B2
Source datasetuspto-grants-2006_10
ORD IDord-14e3682b51c9486fbe7074152353caca
Source noteuspto-grants-2006_10